Project Manager – Companion Diagnostics
Agilent Technologies
full-time
Posted on:
Location Type: Remote
Location: Remote • California • 🇺🇸 United States
Visit company websiteSalary
💰 $100,323 - $156,755 per year
Job Level
Mid-LevelSenior
Tech Stack
PMP
About the role
- Independently coordinate and lead global, cross-functional project teams in a matrix organization with minimal guidance from the Program Manager.
- Some assignments may include projects of greater complexity.
- Demonstrate accountability and urgency to define, drive execution, and deliver expected results according to agreed project scope, requirements, cost, quality and timelines.
- Establish yourself as the primary point-of-contact for key leaders and stakeholders across multiple business units.
- Plan, analyze and track project activities to identify issues and minimize delays, raise as appropriate.
- Estimate and track project costs; proactively communicating deviations to relevant stakeholders.
- Apply appropriate risk management techniques to ensure timelines, business priorities and quality standards are met.
- Use standardized organizational tools, systems and techniques for tracking project progress, maintain current project Gantt charts and task lists.
- Organize and lead team meetings with detailed agendas, clearly documenting meeting minutes, action items, issues, risks and decisions.
- Drive project strategy decisions with Senior Leadership teams; demonstrating an ability to influence at multiple levels.
- Execute multiple projects simultaneously, some being complex, and successfully multi-task amongst several competing initiatives.
Requirements
- Bachelor’s or Advanced degree or University degree or equivalent in biological sciences or a related field.
- Minimum 4 years project management experience in the diagnostic, medical device, pharmaceutical or biotech industry.
- Experience in clinical biomarker or In Vitro Diagnostic development.
- Experience in companion diagnostic development, analytical and clinical validations and regulatory submissions a plus.
- Experience in a regulated industry ( e.g. FDA 21 CFR part 820, ISO 13485, ISO 9001).
- Clear verbal and written communications for a wide variety of audiences.
- Experience with Office Timeline is a plus.
- Experience with Planisware is a plus.
- Experience with IHC is a plus.
- Experience with companion diagnostics is a plus.
- PMP is a plus.
Benefits
- eligibility for bonus
- stock
- benefits
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
project managementrisk managementcost estimationclinical biomarker developmentIn Vitro Diagnostic developmentcompanion diagnostic developmentanalytical validationclinical validationregulatory submissionsmulti-tasking
Soft skills
accountabilityurgencycommunicationinfluenceleadershiporganizationproblem-solvingteam coordinationstakeholder managementmeeting facilitation
Certifications
PMP